ncbi / magicblastLinks
☆36Updated 7 months ago
Alternatives and similar repositories for magicblast
Users that are interested in magicblast are comparing it to the libraries listed below
Sorting:
- Error correction for Illumina RNA-seq reads☆67Updated last year
- PERF is an Exhaustive Repeat Finder☆34Updated 4 years ago
- Ococo: the first online variant and consensus caller. Call genomic consensus directly from an unsorted SAM/BAM stream.☆46Updated 6 years ago
- Master of Pores 2☆23Updated last year
- A collection of publications on comparison of high-throughput sequencing technologies.☆27Updated last week
- Histosketching Using Little Kmers☆56Updated 2 years ago
- A toolkit for annotation of transposable element families from unassembled sequence reads☆30Updated 2 years ago
- Malleable All-seeing Journal Of Research Artifacts☆35Updated 2 years ago
- A pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies☆35Updated last year
- Reference-free variant discovery in large eukaryotic genomes☆41Updated 4 years ago
- Deprecated see https://github.com/MHH-RCUG/nf_wochenende : A whole Genome/Metagenome Sequencing Alignment Pipeline in Python3☆37Updated 3 years ago
- Symmetric DUST for finding low-complexity regions in DNA sequences☆45Updated 4 months ago
- Hitting associations with k-mers☆44Updated 3 years ago
- Find Unique genomic Regions☆32Updated last month
- Ultra-efficient taxonomic mapping of NGS data☆51Updated 4 years ago
- Please see https://github.com/chanzuckerberg/czid-workflows for the latest version of CZ ID workflows.☆27Updated 3 years ago
- Genome guided re-segmention and visualization for raw nanopore sequencing data.☆47Updated 6 years ago
- small RNA analysis from NGS data☆37Updated last year
- full taxonomer cython repository☆22Updated 6 years ago
- A tool for simulating random mutations in any genome☆43Updated last year
- Assembler for raw de novo genome assembly of long uncorrected reads.☆36Updated 5 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆59Updated 8 years ago
- De novo transcriptome assembler for short reads☆64Updated 7 years ago
- REINDEER REad Index for abuNDancE quERy☆56Updated 5 months ago
- utilities for indexing and sequence extraction from FASTA files☆59Updated 4 years ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 3 years ago
- This repository contains the source code of JUDI, a workflow management system for developing complex bioinformatics software with many p…☆33Updated 3 years ago
- http://www.combio.pl/alfree☆23Updated 3 years ago
- This repository has been archived, currently maintained version is at https://github.com/iii-companion/companion☆21Updated 4 years ago
- MIRROR OF: The European Molecular Biology Open Software Suite (from git://anonscm.debian.org/debian-med/emboss.git)☆29Updated 3 years ago